Skip to main content

Contact Us

What are you looking for?

Get in Touch

.
Home
  • Get in Touch
  •  
  • Solutions
    Medicinal Products
    Medical Devices
    Consumer
    Freyr Digital
    Medicinal Products Regulatory Services
    Regulatory Affairs
    Regulatory Operations
    Regulatory Medical Writing
    Regulatory Pharmacovigilance
    Medical and Scientific Communication
    Compliance, Audit, and Validation
    Global Regulatory Intelligence
    • MPR - Regulatory Affairs Menu Block
      • Drug Development Regulatory Services
      • Regulatory Strategy and Insights
      • Dossier Authoring
      • Post Approval/Lifecycle Management
      • Country-specific Regulatory Services
      • Global Health Authorities-Specific Services
      • EU CTR Submissions
    • MPR - Regulatory Operations Menu
      • Regulatory Publishing and Submissions
      • Regulatory Labeling Services
      • Regulatory Artwork Services
    • MPR - Medical Writing Menu Block
      • Clinical Services
      • Non-clinical Services
      • Regulatory Toxicology Services
      • Clinical and Non-Clinical Consulting and Strategic Services
      • Automation in Medical Writing
    • MPR - Pharmacovigilance Menu Block
      • Literature Monitoring
      • ICSR Management
      • Aggregate Reporting
      • Pharmacovigilance Risk Management
      • Signal Management
      • Audit Support and Training Compliance
      • Quality Assurance and Analysis
      • Local Safety Representation
      • Safety Regulatory Intelligence
      • Database Services & Technology Solutions
    • MPR - Medical & Scientific Communication Menu Block
      • Manuscripts and Publications
      • Promotional and Non-promotional Content Curation
      • Creative Scientific Design Studio
      • Promotional Materials Review - MLR
      • FDA Ad Promo Submissions - OPDP 2253
      • Content Management
    • MPR - Compliance and Audit Services Menu Block
      • CAS Consulting
      • SOP Development
      • GxP Audit
      • CSV and CSA
      • QMS Remediation & Establishment
      • End-to-end Compliance Services
    • MPR - GRI Menu Blocks
      • Global Regulatory Intelligence
    Medical Devices Regulatory Services
    Market Access
    Regulatory Affairs
    Clinical & Performance Evaluation
    Quality, Compliance, & Audit
    Digital Health
    Human Factors Engineering
    Global Regulatory Intelligence
    • MDV - Market Access menu block
      • Device Registration Americas
      • Device Registration Europe
      • Device Registration China
      • Device Registration Japan
      • Device Registration South Korea
      • Device Registration Australia
      • Device Registration: Rest of the World
      • In-Country Representation
    • MDV - Regulatory affairs services menu block
      • Translation Support
      • Device Documentation
      • Labeling Services
      • Artwork Services
      • Technical Writing Services
      • RA Staff Augementation Services
      • Regulatory Consulting
    • MDV - Medical Writing services menu block
      • Clinical Evaluation
      • Performance Evaluation
      • Post Market Surveillance
      • Lifecycle Management
      • Literature Search Protocol and Review
    • MDV - Quality Management System services menu block
      • ISO 13485 Certification
      • MDSAP
      • FDA 21 CFR Part 820 Quality System Regulation (QSR)
      • ISO 14971 Risk Management Consulting
    • MDV - Digital Health/SaMD services menu block
      • SaMD Registration in the US
      • SaMD Registration in the EU
      • Australia TGA Software as Medical Devices (SaMD) Registration
      • SaMD Registration in South Korea
    • MDV - Human Factors Engineering for Medical Devices menu Block
      • Human Factors Engineering for Medical Devices
    • MDV - GRI Menu Blocks
      • Global Regulatory Intelligence
    Consumers
    Cosmetics
    Food Supplements
    Chemicals
    • COS - Cosmetics services1 Menu
      • Formulation and Ingredient Review
      • Labeling Review
      • Claims Review
      • Safety Assessment And Toxicology
      • Cosmetic Product Information File (PIF)
      • Go-to-market and Legal Representative (LR)
      COS - Cosmetics services2 Menu
      • Cosmetic Testing
      • Modernization of the Cosmetics Regulation Act of 2022 (MoCRA)
      • Cosmetic Regulatory Intelligence
      • Global Regulatory Intelligence
    • FDS - Service1 Menu block
      • Food Product Service
      • Food Product Claims Substantiation
      • Food Labeling Requirements and Claims Review
      • Food Product Dossier Compilation
      • Food Legal Representation
      • Ecolabeling Regulatory Support
      • GMPs for Dietary Supplements
      • Food Regulatory Pathway Reports
      FDS - Service2 Menu block
      • Food Product Compliance
      • Food Ingredient Assessment and Food Formulation Review
      • Food Supplement Classification
      • Food Supplement Registration
      • Alcoholic Beverage Regulatory Compliance
      • EUDR Compliance Services for Food Industry | Freyr Solutions
      FDS - Service3 Menu block
      • Novel Food Registration
      • NDIN/GRAS (US/US FDA)
      • US FDA Food Facility Registration

      Global Regulatory Intelligence

    • CSRA - Chemicals service1 Menu
      • Chemical Data Scouting
      • Chemical Scientific Assessment Reports and Position Paper Report
      • Supply Chain Regulatory Compliance
      • Chemical Packaging Regulations
      • Biocidal Product Disinfectants - Biocidal Product Regulations
      • Regulation of Tobacco Products
      CSRA - Chemicals service2 Menu
      • Ecolabeling Regulatory Support
      • Chemical Safety Data Sheet
      • Pet Care Products Registration
      • General Product Safety Regulation (GPSR)
      • Global REACH Regulatory Compliance
      • Global Regulatory Intelligence
    Freyr Digital
    Stay Ahead of the Curve With Our Innovative Regulatory Software Solutions

    At the heart of Freyr Digital’s suite of Regulatory software prowess lies the knowledge we have gathered over decade. In a world overflowing with data, we navigate with wisdom, carve out new paths with creativity, and drive forward with the most advanced tech solutions. Know More

    • Consumer
    • Medicinal products
      • Regulatory Affairs Services
        • Drug Development Regulatory Services
          • Pre-submission Meetings/HA Interactions
          • Clinical Trial Applications
        • Regulatory Strategy and Insights
          • Regulatory Strategy Consulting
          • Regulatory Submission Roadmaps/Regulatory Intelligence
          • Regulatory Staffing Services
          • Global Regulatory Affairs Services
          • Gap Analysis
          • Artificial Intelligence (AI)-powered Regulatory Services
        • Dossier Authoring
          • CTD Templates
          • End-to-end DMF Registration
        • Post Approval/Lifecycle Management
          • Post-Approval Change Submissions
          • Nitrosamine Impurity Risk Assessment Submissions
        • Country-specific Regulatory Services
        • Global Health Authorities-Specific Services
        • EU CTR Submissions
      • Regulatory Operations
        • Regulatory Publishing and Submissions
          • AI-powered Regulatory Services
          • eCTD Publishing and Submission Services
          • NeeS Submissions
          • Paper Submissions
          • CSR - Report Level Publishing
          • Legacy Conversions
          • AD promo submission services
          • Archiving Services for Regulatory Publishing and Submission
          • Data Migration Services for Regulatory Publishing and Submission
          • Document Formatting
          • Submission QC Automation
          • Auto Document Level Publishing
        • Regulatory Labeling Services
          • Strategic Labeling Consulting
          • Labeling Translation
          • Regional Labeling
            • USPI Preparation
            • EUSMPC Preparation
            • ROW Labeling
          • Global Labeling
          • Clinical Labeling
          • Labeling Automation
          • AI-powered Regulatory Labeling Services
          • Pharma Labeling Compliance
        • Regulatory Artwork Services
          • Content to Carton
          • Artwork Studio
            • Packaging Design Template Creation
            • Changes to Existing Artwork
            • Private Label Artwork Services
          • Artwork Review / Quality Check
            • Print proof QC
          • Artwork Lifecycle Coordination
            • End-to-End Artwork Workflow Coordination
          • Packaging Artwork Process Consulting
          • Artwork Management System
            • Artwork Workflow Management
            • Artwork Automation
            • Artwork Regulatory Intelligence
          • Eleaflet/elabel
      • Pharmacovigilance
        • Literature Monitoring
        • ICSR Management
        • Aggregate Reporting
        • Pharmacovigilance Risk Management
        • Signal Management
        • Audit Support and Training Compliance
        • Quality Assurance and Analysis
        • Local Safety Representation
        • Safety Regulatory Intelligence
        • Database Services & Technology Solutions
      • Medical Writing
        • Clinical Services
          • Regulatory Writing Services
          • Clinical Trial and Consulting Services
          • Clinical Trial Audit and Monitoring Services
          • Quality Check and Medical Review of Regulatory Documents
          • Risk-Benefit Analysis
          • Data Transparency Initiatives
        • Non-clinical Services
        • Regulatory Toxicology Services
          • ADE/PDE Determination/Report Services
          • F-Value Reports for Child Resistant Packaging (CRP)
          • Toxicological Risk Assessment (TRA) of Impurities, Extractables and Leachables
          • Environmental Risk Assessment (ERA) of Medicinal Products
        • Clinical and Non-Clinical Consulting and Strategic Services
          • Clinical Writing Consulting and Strategic Services
          • Technical Writing Support for GxP Compliance
          • Business Process Optimization
          • Non-clinical Consulting & Strategic Services
        • Automation in Medical Writing
          • Narrative writing tool
          • Literature review tool
          • Formatting tool
          • Quality review tool
          • End-to-End Medical Writing
      • Compliance and Audit Services
        • CAS Consulting
        • SOP Development
        • GxP Audit
          • Remote and Virtual Audits
        • CSV and CSA
        • QMS Remediation & Establishment
        • End-to-end Compliance Services
      • Medical and Scientific Communication
        • Manuscripts and Publications
        • Promotional and Non-promotional Content Curation
          • Content Development
          • Peer Review and QC
        • Creative Scientific Design Studio
        • Promotional Materials Review - MLR
        • FDA Ad Promo Submissions - OPDP 2253
        • Content Management
      • Global Regulatory Intelligence
        • Global Regulatory Intelligence
    • Medical Devices
      • Market Access
        • Device Registration Americas
          • USA
            • e-Star
            • 513(g)
            • 510(k)
            • Q-submission
            • Pre-market Approval
            • RFD & Pre-RFD
            • UDI and GUDID Solutions for the FDA Compliance
          • Canada
            • Canada ISED Representative Service
            • Medical Device Establishment Licence (MDEL) Solutions for Canada
            • Medical Device Importer Solutions for Compliance in Canada
            • Medical Device Licence (MDL) Solutions for Canada
        • Device Registration Europe
          • EAEU
          • EU MDR
          • EU IVDR
          • Europe
          • UK
          • Switzerland
        • Device Registration China
        • Device Registration Japan
        • Device Registration South Korea
        • Device Registration Australia
        • Device Registration: Rest of the World
        • In-Country Representation
          • Australian TGA Sponsor
          • Korean Registration Holder (KRH)
          • Mexican Registration Holder (MRH)
          • US Agent
          • European Authorized Representative (EAR)
          • Swiss Authorised Representative (CH-Rep)
          • UK Responsible Person (UKRP)
          • Designated Market Authorization Holder (DMAH)
          • China Agent Services
          • Brazil Registration Holder (BRH)
          • Indian Authorization Agent for Medical Device Registration in India
          • In-country representation Rest of the world
      • Regulatory Affairs
        • Translation Support
        • Device Documentation
          • Device History File
          • Device Technical File Publishing
        • Labeling Services
        • Artwork Services
        • Technical Writing Services
        • RA Staff Augementation Services
        • Regulatory Consulting
          • Life cycle management
          • Medical Device Consulting
          • IVD Consulting
          • SaMD Consulting
          • Combination product Consulting
          • Regulatory Intelligence
          • Device classification & Categorization
      • Clinical and Performance Evaluation
        • Clinical Evaluation
          • Clinical Evaluation Plan (CEP)
          • Clinical evaluation report (CER)
        • Performance Evaluation
          • Scientific Validity Report (SVR)
          • Clinical Performance Report (CPR)
          • Analytical Performance Report (APR)
          • Performance Evaluation for In Vitro Diagnostic Medical Devices
          • Performance EvaluationReport (PER) IVDR
        • Post Market Surveillance
          • Post-Market Surveillance (PMS)
          • Periodic Safety Update Report (PSUR)
        • Lifecycle Management
        • Literature Search Protocol and Review
      • Quality, Compliance, and Audit
        • ISO 13485 Certification
        • MDSAP
        • FDA 21 CFR Part 820 Quality System Regulation (QSR)
        • ISO 14971 Risk Management Consulting
      • Digital Health
        • SaMD Registration in the US
        • SaMD Registration in the EU
        • Australia TGA Software as Medical Devices (SaMD) Registration
        • SaMD Registration in South Korea
      • Human Factors Engineering for Medical Devices
        • Human Factors Engineering for Medical Devices
      • Global Regulatory Intelligence
        • Global Regulatory Intelligence
    • Cosmetics
      • Cosmetics Services
        • Formulation and Ingredient Review
        • Labeling Review
        • Claims Review
        • Safety Assessment And Toxicology
        • Cosmetic Product Information File (PIF)
        • Go-to-market and Legal Representative (LR)
      • Cosmetics Service
        • Cosmetic Testing
        • Modernization of the Cosmetics Regulation Act of 2022 (MoCRA)
        • Cosmetic Regulatory Intelligence
        • Global Regulatory Intelligence
    • Food Supplements
      • Food Product Service
        • Food Product Service
        • Food Product Claims Substantiation
        • Food Labeling Requirements and Claims Review
        • Food Product Dossier Compilation
        • Food Legal Representation
        • Ecolabeling Regulatory Support
        • GMPs for Dietary Supplements
        • Food Regulatory Pathway Reports
      • Food Product Compliance
        • Food Product Compliance
        • Food Ingredient Assessment and Food Formulation Review
        • Food Supplement Classification
        • Food Supplement Registration
        • Alcoholic Beverage Regulatory Compliance
        • EUDR Compliance Services for Food Industry | Freyr Solutions
      • Novel Food Registration
        • Novel Food Registration
        • NDIN/GRAS (US/US FDA)
        • US FDA Food Facility Registration
    • Chemicals
      • CSRA Services
        • Chemical Data Scouting
        • Chemical Scientific Assessment Reports and Position Paper Report
        • Supply Chain Regulatory Compliance
        • Chemical Packaging Regulations
        • Biocidal Product Disinfectants - Biocidal Product Regulations
        • Regulation of Tobacco Products
      • CSRA Services
        • Ecolabeling Regulatory Support
        • Chemical Safety Data Sheet
        • Pet Care Products Registration
        • General Product Safety Regulation (GPSR)
        • Global REACH Regulatory Compliance
        • Global Regulatory Intelligence
  • Global
    Americas
    Europe
    Asia-Pacific
    Africa & Middle East
    Global Americas Menu Block
    • Argentina
    • Bolivia
    • Brazil
    • Canada
    • Chile
    • Colombia
    • Costa Rica
    • Dominican Republic
    • Guatemala
    • Mexico
    • Panama
    • Paraguay
    • Peru
    • Puerto Rico
    • United States
    • Venezuela
    Global Europe Menu Block
    • Albania
    • Austria
    • Belarus
    • Belgium
    • Bulgaria
    • Croatia
    • Cyprus
    • Czech Republic
    • Denmark
    • Estonia
    • European Union
    • Finland
    • France
    • Germany
    • Greece
    • Hungary
    • Ireland
    • Italy
    • Kazakhstan
    • Kosovo
    • Latvia
    • Lithuania
    • Luxembourg
    • Macedonia
    • Malta
    • Netherlands
    • Norway
    • Poland
    • Portugal
    • Romania
    • Serbia
    • Slovakia
    • Slovenia
    • Spain
    • Sweden
    • Switzerland
    • United Kingdom
    • Uzbekistan
    Global Asia - Pacific Menu Block
    • Australia
    • Bangladesh
    • Cambodia
    • China
    • Hong Kong
    • India
    • Indonesia
    • Japan
    • Malaysia
    • New Zealand
    • Pakistan
    • Philippines
    • Russia
    • Singapore
    • South Korea
    • Sri Lanka
    • Taiwan
    • Thailand
    • Vietnam
    Global Africa & Middle East Menu Block
    • Algeria
    • Bahrain
    • Egypt
    • Ethiopia
    • Ghana
    • Iraq
    • Israel
    • Jordan
    • Kenya
    • Lebanon
    • Morocco
    • Nigeria
    • Qatar
    • Saudi Arabia
    • South Africa
    • Tunisia
    • Turkey
    • UAE
    • Uganda
    • Yemen
    • Zimbabwe
    • kuwait
    • Americas
      • Argentina
      • Bolivia
      • Brazil
      • Canada
      • Chile
      • Colombia
      • Costa Rica
      • Dominican Republic
      • Guatemala
      • Mexico
      • Panama
      • Paraguay
      • Peru
      • Puerto Rico
      • United States
      • Venezuela
    • Europe
      • Albania
      • Austria
      • Belarus
      • Belgium
      • Bulgaria
      • Croatia
      • Cyprus
      • Czech Republic
      • Denmark
      • Estonia
      • Finland
      • France
      • Germany
      • European Union
      • Greece
      • Hungary
      • Ireland
      • Italy
      • Kazakhstan
      • Kosovo
      • Latvia
      • Lithuania
      • Luxembourg
      • Macedonia
      • Malta
      • Netherlands
      • Norway
      • Poland
      • Portugal
      • Romania
      • Serbia
      • Slovakia
      • Slovenia
      • Spain
      • Sweden
      • Switzerland
      • United Kingdom
      • Uzbekistan
    • Asia-Pacific
      • Australia
      • Bangladesh
      • Cambodia
      • China
      • Hong Kong
      • India
      • Indonesia
      • Japan
      • Malaysia
      • New Zealand
      • Pakistan
      • Philippines
      • Russia
      • Singapore
      • South Korea
      • Sri Lanka
      • Taiwan
      • Thailand
      • Vietnam
    • Africa & Middle East
      • Algeria
      • Bahrain
      • Egypt
      • Ethiopia
      • Ghana
      • Iraq
      • Israel
      • Jordan
      • Kenya
      • Lebanon
      • Morocco
      • Nigeria
      • Qatar
      • Saudi Arabia
      • South Africa
      • Tunisia
      • Turkey
      • UAE
      • Uganda
      • Yemen
      • Zimbabwe
      • kuwait
  • Customers
    • Success Stories Success Redefined, Stories Retold
    • Case Studies Real-world Impact, Detailed in Every Study
    • Testimonials Voices of Trust, Stories of Satisfaction
  • Insights
    • Blogs Daily Dose of Various Regulatory Perspectives
    • Brochures Segment-wise Service Portfolios Charted
    • Infographics Brief and Informative Visual Guides on Regulatory Aspects
    • Webinars Presenting Expert Opinions in an Insightful Way
    • Freyr Podcasts Expert Regulatory Discussions from Industry Leaders
    • Expert Insights Unveiling Expertise, Shaping Perspectives
    • What is ...? Life Sciences Regulatory Glossary Explained
    • White Papers Comprehensive and Clear-cut Regulatory Opinions
    • e-Books Regulatory Subject and Topic-specific Booklets
    • Global Health Authority Mandates With respect to Global Life Sciences and Med Tech Industries
    • Regulatory Roundup Weekly Regulatory News from Global Health Authorities
    • Templates and Checklists Streamline Success with Templates & Checklists
    • Industry News
    • Videos
    • Toolkits
  • Company
    • About Us Our Story: Passion, Purpose, Progress
    • Awards & Recognitions Proud Moments, Endless Gratitude
    • Press Releases All About Freyr Releases, Achievements and Accolades
    • Freyr in Media The Outlook of Freyr and Series of Publications
    • Industry Events Whereabouts of Freyr, as an Industry Expert
    • Compliance Wall Guardians of Integrity, Defenders of Compliance
    • Corporate Social Responsibility Destined to Enrich the Society and the Humankind
    • Functional Delivery Models Announcing Excellence, Inspiring Impact
    • Careers Be a Part of the Journey
    • Partner with Us Empower Your Regulatory Journey
    • Contact Us Connecting You to Solutions, One Click Away
  • Get in Touch
  •  English
    • Japan (Japanese | English)
    • South Korea (Korean | English)
    • China (Chinese | English)
    • Mexico (Español | English)
    • Brazil (Portuguese | English)
    • Australia (English)
    • Sri Lanka (English)
    • India (English)
    • Malaysia (English)
    • Nigeria (English)
    • Saudi Arabia (English)
    • Thailand (English)
  •  
  •  
    • +1 908 483 7958
    • +44 2037 012379
    • +1 778 308 4671
    • +49 6181 707 9007
    • +52 55 41613365
    • +65 315 894 72
    • +60 39 212 5527
    • +91 40 4848 0999
    • +61 2 8607 5105
    • +41 225 087 129
  •  
    • sales@freyrsolutions.com
    • hr@freyrsolutions.com

Breadcrumb

  1. Home
  2. Food Industry News
  3. EU Included 2-hydroxy-4-methoxybenzaldehyde As a Food Flavoring Substance

EU included 2-hydroxy-4-methoxybenzaldehyde as a food flavoring substance

March 1, 2023

EU amended the Annex I to Regulation (EC) No 1334/2008 to include 2-hydroxy-4-methoxybenzaldehyde in the Union list of flavourings.

Source:
https://eur-lex.europa.eu/legal-content/EN/TXT/PDF/?uri=CELEX%3A32023R0441
News Region:
European Union
News Market:
European Union
News Tags:
EU
2-hydroxy-4-methoxybenzaldehyde
Food flavouring

Recent Industry News

  • Regulations on Changes to Regulations on Food Additives
  • Thailand releases pre-packaged food labelling regulations
  • Thailand releases new food serial number management implementation regulations
  • South Korea issued a partial revision of the "Food Labeling Standards"
More

How can we help you?

Please let us know your requirements, and we will contact you.
  +1 908 483 7958
  +44 203 701 2379
  +91 40 4848 0999
  +27 105 002 556

  sales@freyrsolutions.com


Connect with Us

  •  

  •  
  •  
  •  
Terms of Use | Privacy Policy | Cookie Policy | Customize Cookies
© Copyright 2024 Freyr. All Rights Reserved.
  •  
  •  
  •  
  • Home
  • Solutions
    • Back
    • Solutions
    • Medicinal Products
      • Back
      • Medicinal Products Regulatory Services

        Regulatory Affairs
        Regulatory Operations
        Regulatory Medical Writing
        Regulatory Pharmacovigilance
        Medical and Scientific Communication
        Compliance, Audit, and Validation
        Global Regulatory Intelligence
        • MPR - Regulatory Affairs Menu Block
          • Drug Development Regulatory Services
          • Regulatory Strategy and Insights
          • Dossier Authoring
          • Post Approval/Lifecycle Management
          • Country-specific Regulatory Services
          • Global Health Authorities-Specific Services
          • EU CTR Submissions
        • MPR - Regulatory Operations Menu
          • Regulatory Publishing and Submissions
          • Regulatory Labeling Services
          • Regulatory Artwork Services
        • MPR - Medical Writing Menu Block
          • Clinical Services
          • Non-clinical Services
          • Regulatory Toxicology Services
          • Clinical and Non-Clinical Consulting and Strategic Services
          • Automation in Medical Writing
        • MPR - Pharmacovigilance Menu Block
          • Literature Monitoring
          • ICSR Management
          • Aggregate Reporting
          • Pharmacovigilance Risk Management
          • Signal Management
          • Audit Support and Training Compliance
          • Quality Assurance and Analysis
          • Local Safety Representation
          • Safety Regulatory Intelligence
          • Database Services & Technology Solutions
        • MPR - Medical & Scientific Communication Menu Block
          • Manuscripts and Publications
          • Promotional and Non-promotional Content Curation
          • Creative Scientific Design Studio
          • Promotional Materials Review - MLR
          • FDA Ad Promo Submissions - OPDP 2253
          • Content Management
        • MPR - Compliance and Audit Services Menu Block
          • CAS Consulting
          • SOP Development
          • GxP Audit
          • CSV and CSA
          • QMS Remediation & Establishment
          • End-to-end Compliance Services
        • MPR - GRI Menu Blocks
          • Global Regulatory Intelligence

    • Medical Devices
      • Back
      • Medical Devices Regulatory Services

        Market Access
        Regulatory Affairs
        Clinical & Performance Evaluation
        Quality, Compliance, & Audit
        Digital Health
        Human Factors Engineering
        Global Regulatory Intelligence
        • MDV - Market Access menu block
          • Device Registration Americas
          • Device Registration Europe
          • Device Registration China
          • Device Registration Japan
          • Device Registration South Korea
          • Device Registration Australia
          • Device Registration: Rest of the World
          • In-Country Representation
        • MDV - Regulatory affairs services menu block
          • Translation Support
          • Device Documentation
          • Labeling Services
          • Artwork Services
          • Technical Writing Services
          • RA Staff Augementation Services
          • Regulatory Consulting
        • MDV - Medical Writing services menu block
          • Clinical Evaluation
          • Performance Evaluation
          • Post Market Surveillance
          • Lifecycle Management
          • Literature Search Protocol and Review
        • MDV - Quality Management System services menu block
          • ISO 13485 Certification
          • MDSAP
          • FDA 21 CFR Part 820 Quality System Regulation (QSR)
          • ISO 14971 Risk Management Consulting
        • MDV - Digital Health/SaMD services menu block
          • SaMD Registration in the US
          • SaMD Registration in the EU
          • Australia TGA Software as Medical Devices (SaMD) Registration
          • SaMD Registration in South Korea
        • MDV - Human Factors Engineering for Medical Devices menu Block
          • Human Factors Engineering for Medical Devices
        • MDV - GRI Menu Blocks
          • Global Regulatory Intelligence

    • Cosmetics
      • Back
      • Cosmetics Regulatory Services

        COS - Cosmetics services1 Menu
        • Formulation and Ingredient Review
        • Labeling Review
        • Claims Review
        • Safety Assessment And Toxicology
        • Cosmetic Product Information File (PIF)
        • Go-to-market and Legal Representative (LR)
        COS - Cosmetics services2 Menu
        • Cosmetic Testing
        • Modernization of the Cosmetics Regulation Act of 2022 (MoCRA)
        • Cosmetic Regulatory Intelligence
        • Global Regulatory Intelligence

    • Food Supplements
      • Back
      • Food Supplements Regulatory Services
        Food Product Service

        FDS - Food Product Service menu
        • Food Product Service
        • Food Product Claims Substantiation
        • Food Labeling Requirements and Claims Review
        • Food Product Dossier Compilation
        • Food Legal Representation
        • Ecolabeling Regulatory Support
        • GMPs for Dietary Supplements
        • Food Regulatory Pathway Reports

        Food Product Compliance

        FDS - Food Product Compliance Menu
        • Food Product Compliance
        • Food Ingredient Assessment and Food Formulation Review
        • Food Supplement Classification
        • Food Supplement Registration
        • Alcoholic Beverage Regulatory Compliance
        • EUDR Compliance Services for Food Industry | Freyr Solutions

        Novel Food Registration

        FDS - Novel Food Registration Menu
        • Novel Food Registration
        • NDIN/GRAS (US/US FDA)
        • US FDA Food Facility Registration

    • Chemicals
      • Back
      • Chemicals Regulatory Services

        CSRA - Chemicals service1 Menu
        • Chemical Data Scouting
        • Chemical Scientific Assessment Reports and Position Paper Report
        • Supply Chain Regulatory Compliance
        • Chemical Packaging Regulations
        • Biocidal Product Disinfectants - Biocidal Product Regulations
        • Regulation of Tobacco Products
        CSRA - Chemicals service2 Menu
        • Ecolabeling Regulatory Support
        • Chemical Safety Data Sheet
        • Pet Care Products Registration
        • General Product Safety Regulation (GPSR)
        • Global REACH Regulatory Compliance
        • Global Regulatory Intelligence

  • Global
    • Back
    • Global
    • Americas
      • Back
      • Americas
      • Mobile Menu Americas
        • Argentina
        • Bolivia
        • Brazil
        • Canada
        • Chile
        • Colombia
        • Costa Rica
        • Dominican Republic
        • Guatemala
        • Mexico
        • Panama
        • Paraguay
        • Peru
        • Puerto Rico
        • United States
        • Venezuela
    • Eupope
      • Back
      • Eupope
      • Mobile Menu Eupope
        • Albania
        • Austria
        • Belarus
        • Belgium
        • Bulgaria
        • Croatia
        • Cyprus
        • Czech Republic
        • Denmark
        • Estonia
        • European Union
        • Finland
        • France
        • Germany
        • Greece
        • Hungary
        • Ireland
        • Italy
        • Kazakhstan
        • Kosovo
        • Latvia
        • Lithuania
        • Luxembourg
        • Macedonia
        • Malta
        • Netherlands
        • Norway
        • Poland
        • Portugal
        • Romania
        • Serbia
        • Slovakia
        • Slovenia
        • Spain
        • Sweden
        • Switzerland
        • United Kingdom
        • Uzbekistan
    • Asia - Pacific
      • Back
      • Asia - Pacific
      • Mobile Menu Asia - Pacific
        • Australia
        • Bangladesh
        • Cambodia
        • China
        • Hong Kong
        • India
        • Indonesia
        • Japan
        • Malaysia
        • New Zealand
        • Pakistan
        • Philippines
        • Russia
        • Singapore
        • South Korea
        • Sri Lanka
        • Taiwan
        • Thailand
        • Vietnam
    • Africa & Middle East
      • Back
      • Africa & Middle East
      • Mobile Menu Africa & Middle East
        • Algeria
        • Bahrain
        • Egypt
        • Ethiopia
        • Ghana
        • Iraq
        • Israel
        • Jordan
        • Kenya
        • Lebanon
        • Morocco
        • Nigeria
        • Qatar
        • Saudi Arabia
        • South Africa
        • Tunisia
        • Turkey
        • UAE
        • Uganda
        • Yemen
        • Zimbabwe
        • kuwait
  • Customers
    • Back
    • Customers
    • Mobile Menu Customers
      • Success Stories
      • Case Studies
      • Testimonials
  • Insights
    • Back
    • Insights
    • Mobile Menu Insights
      • Blogs
      • Brochures
      • Infographics
      • Webinars
      • Freyr Podcasts
      • Expert Insights
      • What is ...?
      • White Papers
      • e-Books
      • Global Health Authority Mandates
      • Regulatory Roundup
      • Templates and Checklists
      • Industry News
      • Videos
      • Toolkits
  • Company
    • Back
    • Company
    • Mobile Menu Company
      • About Us
      • Awards & Recognitions
      • Press Releases
      • Freyr in Media
      • Industry Events
      • Compliance Wall
      • Corporate Social Responsibility
      • Functional Delivery Models
      • Careers
      • Partner with Us
      • Contact Us

  •  

    • Japan Japanese | English
    • South Korea Korean | English
    • China Chinese | English
    • Mexico Español | English
    • Brazil Portuguese | English
    • Australia English
    • Sri Lanka English
    • India English
    • Malaysia English
    • Nigeria English
    • Saudi Arabia English
    • Thailand English

×